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大沸石 H-ZSM-5 晶体作为甲醇制烃过程的模型:弥合单颗粒研究与整体催化剂分析之间的差距。

Large zeolite H-ZSM-5 crystals as models for the methanol-to-hydrocarbons process: bridging the gap between single-particle examination and bulk catalyst analysis.

机构信息

Inorganic Chemistry and Catalysis, Debye Institute for Nanomaterials Science, Utrecht University, Universiteitsweg 99, 3584 CG Utrecht, The Netherlands.

出版信息

Chemistry. 2013 Jun 24;19(26):8533-42. doi: 10.1002/chem.201203351. Epub 2013 May 6.

DOI:10.1002/chem.201203351
PMID:23649944
Abstract

The catalytic, deactivation, and regeneration characteristics of large coffin-shaped H-ZSM-5 crystals were investigated during the methanol-to-hydrocarbons (MTH) reaction at 350 and 500 °C. Online gas-phase effluent analysis and examination of retained material thereof were used to explore the bulk properties of large coffin-shaped zeolite H-ZSM-5 crystals in a fixed-bed reactor to introduce them as model catalysts for the MTH reaction. These findings were related to observations made at the individual particle level by using polarization-dependent UV-visible microspectroscopy and mass spectrometric techniques after reaction in an in situ microspectroscopy reaction cell. Excellent agreement between the spectroscopic measurements and the analysis of hydrocarbon deposits by means of retained hydrocarbon analysis and time-of-flight secondary-ion mass spectrometry of spent catalyst materials was observed. The obtained data reveal a shift towards more condensed coke deposits on the outer zeolite surface at higher reaction temperatures. Zeolites in the fixed-bed reactor setup underwent more coke deposition than those reacted in the in situ microspectroscopy reaction cell. Regeneration studies of the large zeolite crystals were performed by oxidation in O2 /inert gas mixtures at 550 °C. UV-visible microspectroscopic measurements using the oligomerization of styrene derivatives as probe reaction indicated that the fraction of strong acid sites decreased during regeneration. This change was accompanied by a slight decrease in the initial conversion obtained after regeneration. H-ZSM-5 deactivated more rapidly at higher reaction temperature.

摘要

研究了在 350 和 500°C 下甲醇制烃(MTH)反应中大型棺材形 H-ZSM-5 晶体的催化、失活和再生特性。在线气相流出物分析和保留物的检查用于探索固定床反应器中大型棺材形沸石 H-ZSM-5 晶体的体相性质,将其作为 MTH 反应的模型催化剂。这些发现与使用偏振相关的紫外可见微光谱和原位微光谱反应池中反应后的质谱技术在单个颗粒水平上的观察结果相关。通过保留烃分析和用过的催化剂材料的飞行时间二次离子质谱对烃沉积物的分析,观察到光谱测量与烃沉积物的分析之间极好的一致性。获得的数据表明,在较高的反应温度下,沸石外表面上的焦炭沉积物向更密集的方向转变。固定床反应器装置中的沸石比在原位微光谱反应池中的沸石沉积更多的焦炭。通过在 550°C 的 O2/惰性气体混合物中氧化对大沸石晶体进行了再生研究。使用苯乙烯衍生物的齐聚作为探针反应的紫外可见微光谱测量表明,在再生过程中强酸位的分数减少。这种变化伴随着再生后初始转化率的轻微下降。在较高的反应温度下,H-ZSM-5 失活更快。

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